Movement Disorder Phenotypes in Children With 22q11.2 Deletion Syndrome

被引：10
|
作者：
Cunningham, Adam C. [1 ]
Fung, Wilson [2 ]
Massey, Thomas H. [1 ]
Hall, Jeremy [1 ,3 ]
Owen, Michael J. [1 ,3 ]
van den Bree, Marianne B. M. [1 ,3 ]
Peall, Kathryn J. [3 ]
机构：
[1] Cardiff Univ, Sch Med, Div Psychol Med & Clin Neurosci, MRC Ctr Neuropsychiat Genet & Genom, Cardiff, Wales
[2] Royal Gwent Hosp, Aneurin Bevan Univ Hlth Board, Newport, Gwent, Wales
[3] Cardiff Univ, Sch Med, Div Psychol Med & Clin Neurosci, Neurosci & Mental Hlth Res Inst, Cardiff, Wales
来源：
MOVEMENT DISORDERS | 2020年 / 35卷 / 07期
基金：
英国医学研究理事会; 英国惠康基金;
关键词：
D O I：
10.1002/mds.28078
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：1272 / 1274
页数：3
相关论文
共 50 条
  • [21] Psychosis in children with velocardiofacial syndrome (22q11.2 deletion syndrome)
    Edith M. Jolin
    Ronald A. Weller
    Elizabeth B. Weller
    Current Psychiatry Reports, 2009, 11 : 99 - 105
  • [22] 22q11.2 deletion syndrome and schizophrenia
    Qin, Xianzheng
    Chen, Jiang
    Zhou, Tian
    ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2020, 52 (11) : 1181 - 1190
  • [23] Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome
    Heung, Tracy
    Conroy, Brigid
    Malecki, Sarah
    Ha, Joanne
    Boot, Erik
    Corral, Maria
    Bassett, Anne S.
    GENES, 2022, 13 (11)
  • [24] Camptodactyly and the 22q11.2 deletion syndrome
    Couser, Natario L.
    Pande, Chetna K.
    Walsh, Jonathan M.
    Tepperberg, James
    Aylsworth, Arthur S.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (02) : 515 - 518
  • [25] Schizophrenia and 22q11.2 deletion syndrome
    Bassett A.S.
    Chow E.W.C.
    Current Psychiatry Reports, 2008, 10 (2) : 148 - 157
  • [26] Coexisting Conditions Modifying Phenotypes of Patients with 22q11.2 Deletion Syndrome
    Smyk, Marta
    Geremek, Maciej
    Ziemkiewicz, Kamila
    Gambin, Tomasz
    Kutkowska-Kazmierczak, Anna
    Kowalczyk, Katarzyna
    Plaskota, Izabela
    Wisniowiecka-Kowalnik, Barbara
    Bartnik-Glaska, Magdalena
    Niemiec, Magdalena
    Grad, Dominika
    Piotrowicz, Malgorzata
    Gieruszczak-Bialek, Dorota
    Pietrzyk, Aleksandra
    Crowley, T. Blaine
    Giunta, Victoria
    McGinn, Daniel E.
    Zackai, Elaine H.
    Tran, Oanh
    Emanuel, Beverly S.
    McDonald-McGinn, Donna M.
    Nowakowska, Beata A.
    GENES, 2023, 14 (03)
  • [27] Coexisting conditions modifying phenotypes of patients with 22q11.2 Deletion Syndrome
    Geremek, Maciej
    Smyk, Marta
    Kutkowska-Kazmierczak, Anna
    Ziemkiewicz, Kamila
    Gambin, Tomasz
    Crowley, T. Blaine
    Zackai, Elaine
    Emanuel, Beverly
    McDonald-McGinn, Donna
    Nowakowska, Beata
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 237 - 237
  • [28] 22q11.2 deletion syndrome: Introduction
    Lajiness-O'Neill, R
    CHILD NEUROPSYCHOLOGY, 2005, 11 (01) : 1 - 3
  • [29] Differences in speech and language abilities between children with 22q11.2 deletion syndrome and children with phenotypic features of 22q11.2 deletion syndrome but without microdeletion
    Rakonjac, Marijana
    Cuturilo, Goran
    Stevanovic, Milena
    Jelicic, Ljiljana
    Subotic, Misko
    Jovanovic, Ida
    Drakulic, Danijela
    RESEARCH IN DEVELOPMENTAL DISABILITIES, 2016, 55 : 322 - 329
  • [30] Anomalies of the genitourinary tract in children with 22q11.2 deletion syndrome
    Van Batavia, Jason P.
    Crowley, Terrence B.
    Burrows, Evanette
    Zackai, Elaine H.
    Sanna-Cherchi, Simone
    McDonald-McGinn, Donna M.
    Kolon, Thomas F.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2019, 179 (03) : 381 - 385
12345